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Thermo Fisher Scientific PAX6 Polyclonal Antibody
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Thermo Fisher Scientific PAX6 Polyclonal Antibody

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PAX6 단백질을 검출하기 위한 Thermo Fisher Scientific의 폴리클로날 항체. 인간, 마우스, 랫트 시료에 반응하며 WB, IHC, ICC/IF, Flow Cytometry 등에 사용 가능. 액상 형태로 제공되며 -20°C에서 보관. 연구용으로만 사용 가능.

카탈로그번호
426600
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 11:48
Thermo Fisher Scientific 426600 PAX6 Polyclonal Antibody 100 ug pk판매 단위 pk ·
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627,600원VAT 포함 690,360원

Thermo Fisher Scientific · Thermo Fisher Scientific PAX6 Polyclonal Antibody

Thermo Fisher Scientific PAX6 Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution Publications
Western Blot (WB) 1–2 µg/mL 4 publications
Immunohistochemistry (IHC) 11 publications
Immunohistochemistry (Paraffin) (IHC (P)) 1:100
Immunohistochemistry (PFA fixed) (IHC (PFA)) 1 publication
Immunohistochemistry (Frozen) (IHC (F)) Assay-dependent 1 publication
Immunocytochemistry (ICC/IF) 2–3 µg/mL 12 publications
Flow Cytometry (Flow) 1:100 1 publication
Immunoprecipitation (IP) 1 publication
Miscellaneous PubMed (Misc) 1 publication

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Published Species Human, Mouse, Rat
Host/Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Human Pax6
Conjugate Unconjugated
Form Liquid
Concentration 0.25 mg/mL
Purification Affinity chromatography
Storage Buffer PBS, pH 7.4
Contains 0.1% sodium azide
Storage Conditions -20°C
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2533534

Product Specific Information

Antibody 42-6600 has been successfully used in flow cytometry and immunofluorescence analysis of Pax6 in human neural stem cells derived from pluripotent stem cells and reacts with human samples.

Target Information

The PAX6 gene encodes paired box gene 6, a human homolog of the Drosophila melanogaster gene prd. This gene family is characterized by a conserved paired box domain and a homeobox domain, both of which bind DNA and regulate gene transcription. PAX6 is expressed in the developing nervous system and eyes. Mutations in this gene can cause ocular disorders such as aniridia and Peter’s anomaly. Alternatively spliced transcript variants encoding identical or distinct isoforms have been identified.

Usage Notice

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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